Journal Article PreJuSER-57108

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A Novel Approach to Measure the Step Line Tension and the Step Dipole Moment on Vicinal Au(001) Electrodes

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2007
Elsevier Amsterdam

Surface science 601, 1876 - 1885 () [10.1016/j.susc.2007.02.012]

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Abstract: In this paper we introduce a new experimental approach to determine the potential dependence of the step line tension on metal electrodes in contact with an electrolyte: (0 0 1) and (1 1 n) surfaces of single crystal gold electrodes were investigated by impedance spectroscopy in solutions containing weakly adsorbing anions, such as CIO4-, F- and SO42-. Within the limits of error the shift in the potential of zero charge is proportional to the step density of the vicinal surfaces indicative of a well-defined dipole moment per step length. The dipole moments per step atom are 6.8 +/- 0.8, 5.2 +/- 0.4, 5.8 +/- 0.5 x 10(-3) e angstrom for SO42-, ClO4-, and F- containing electrolytes, respectively. Using the values for the pzc and the potential dependence of the capacitance curves, the potential dependence of the surface tension of the vicinal surfaces is determined. The line tension of the steps is then calculated from the difference between the surface tension of the stepped and the step free surface. Our results represent the first experimental confirmation of a recent theoretical model proposing that in absence of specifically adsorbed ions the step line tension should decrease (roughly linear) with potential. (c) 2007 Elsevier B.V. All rights reserved.

Keyword(s): J ; stepped electrodes (auto) ; vicinal (auto) ; STM (auto) ; step line tension (auto) ; step dipole moment (auto) ; potential of zero charge (auto) ; Au(001) (auto) ; electrolyte (auto)


Note: Record converted from VDB: 12.11.2012

Contributing Institute(s):
  1. Biomechanik (IBN-4)
  2. Grenz- und Oberflächen (IBN-3)
  3. Jülich-Aachen Research Alliance - Fundamentals of Future Information Technology (JARA-FIT)
Research Program(s):
  1. Kondensierte Materie (P54)

Appears in the scientific report 2007
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 Datensatz erzeugt am 2012-11-13, letzte Änderung am 2020-04-02



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